Severe Necrotizing Anterior Scleritis in Marfan Syndrome: A Case of Scleromalacia Perforans
Mehrdad Motamed Shariati, Sara Ghafari
TL;DR
This paper presents a rare case of severe eye inflammation in a patient with Marfan Syndrome, highlighting the need for aggressive treatment.
Contribution
The novelty lies in documenting scleromalacia perforans as a rare manifestation of Marfan Syndrome.
Findings
Severe necrotizing anterior scleritis occurred in a patient with Marfan Syndrome.
The condition required aggressive treatment to prevent permanent vision loss.
Abstract
Necrotizing scleritis is considered the most severe form of scleritis. Because of the associated risk of permanent vision loss and potential complications, aggressive treatment, which may include the use of immunosuppressives or intravenous antibiotics, based on the underlying etiology, is essential. Severe necrotizing scleritis.
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Click any figure to enlarge with its caption.
Figure 1
Figure 2Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsDermatological and Skeletal Disorders · Skin Diseases and Diabetes · Ocular Diseases and Behçet’s Syndrome